gudid
Primary ID: SLD
zumax (UDI SLD)
Manufactured by Zumax Medical Co., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for zumax - Primary ID SLD
Device Regulatory Overview
The zumax (Model/Catalog Number: SLD) is a medical device manufactured by Zumax Medical Co., LTD. This product is indexed under FDA Product Code / Category Classification HJH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SLD
- Product Code / EMDN
- HJH
- Device Name
- Database Sync Date
- 2026-08-09 09:11:03
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of zumax?
The registered manufacturer of record for zumax is Zumax Medical Co., LTD.
What is the Primary UDI-DI identifier for zumax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SLD.
What classification code is assigned to this device?
This device is registered under product classification code HJH.
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